FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DAVOL HYSTEROSCOPY POUCH DRAPE AND TUBING SET, MODEL OOXXXXO

K Number: K991799 · Decision Sep 13, 1999
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
55
Applicant Total
24
Review Days
110

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Basic Information

Device Name
DAVOL HYSTEROSCOPY POUCH DRAPE AND TUBING SET, MODEL OOXXXXO
K Number
K991799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1700
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Davol Inc., Sub. C. R. Bard, Inc.
Date Received
May 26, 1999
Decision Date
September 13, 1999
Product Code
HIG
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HIG Insufflator, Hysteroscopic

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Other Clearances by Davol Inc., Sub. C. R. Bard, Inc.

K Number Device Name
K101851 VENTRALIGHT ST MESH
K092032 BARD PERFIX LIGHT PLUG, MODELS 0117050, 0117060, 0117070, 0117080, 0117150, 0117160
K081010 BARD 3DMAX MESH
K061754 BARD COMPOSITE L/P MESH
K061314 BARD EXTRA LARGE COMPOSIX KUGEL HERNIA PATCH
K051848 SALUTE II DISPOSABLE FIXATION DEVICE, MODELS 0113070, 0113072, 0113073, 0113077, 0113079
K050610 SALUTE FIXATION SYSTEM
K011069 AQUASENS FLUID MONITORING SYSTEM
K003674 NEZHAT-DORSEY REUSABLE ELECTROSURGICAL ATTACHMENTS: J-HOOK TIP, L-HOOK TIP, CORBITT SPATULA TIP, NEEDLE TIP, BALL TIP
K991637 BARD SPERMA-TEX PRESHAPED MESH (2.4X5.6), MODEL 0114700
Search all 24 clearances from Davol Inc., Sub. C. R. Bard, Inc. →